EP0261070A1 - Mousses céramiques - Google Patents

Mousses céramiques Download PDF

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Publication number
EP0261070A1
EP0261070A1 EP87630196A EP87630196A EP0261070A1 EP 0261070 A1 EP0261070 A1 EP 0261070A1 EP 87630196 A EP87630196 A EP 87630196A EP 87630196 A EP87630196 A EP 87630196A EP 0261070 A1 EP0261070 A1 EP 0261070A1
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EP
European Patent Office
Prior art keywords
metal
ceramic
oxidant
aluminum
ligaments
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EP87630196A
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German (de)
English (en)
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EP0261070B1 (fr
Inventor
Eugene Sangmoo Park
Steven Douglas Poste
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Rio Tinto Alcan International Ltd
Lanxide Technology Co LP
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Alcan International Ltd Canada
Lanxide Technology Co LP
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Priority claimed from US07/089,376 external-priority patent/US4808558A/en
Application filed by Alcan International Ltd Canada, Lanxide Technology Co LP filed Critical Alcan International Ltd Canada
Priority to AT87630196T priority Critical patent/ATE76050T1/de
Publication of EP0261070A1 publication Critical patent/EP0261070A1/fr
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    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64—Burning or sintering processes
    • C04B35/65—Reaction sintering of free metal- or free silicon-containing compositions
    • C04B35/652—Directional oxidation or solidification, e.g. Lanxide process
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/0022—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof obtained by a chemical conversion or reaction other than those relating to the setting or hardening of cement-like material or to the formation of a sol or a gel, e.g. by carbonising or pyrolysing preformed cellular materials based on polymers, organo-metallic or organo-silicon precursors
    • C04B38/0025—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof obtained by a chemical conversion or reaction other than those relating to the setting or hardening of cement-like material or to the formation of a sol or a gel, e.g. by carbonising or pyrolysing preformed cellular materials based on polymers, organo-metallic or organo-silicon precursors starting from inorganic materials only, e.g. metal foam; Lanxide type products

Definitions

  • the present invention relates to ceramic products having a ceramic skeletal structure, i.e. rigid foams, and, more particularly, to ceramic products having a three-dimensional skeletal structure of randomly interconnected cells or channels.
  • the invention relates also to the method of forming such products.
  • Open-cell ceramic foams are commercially desirable for use in a variety of products including filters for molten metals, diesel particulate traps, catalytic converters for automotive exhaust treatment, heat exchangers, heating elements, thermal and electric insulators, etc.
  • filters for molten metals diesel particulate traps
  • catalytic converters for automotive exhaust treatment heat exchangers
  • heating elements thermal and electric insulators, etc.
  • the high strength-to-weight ratio achievable with ceramic foams is an attractive advantage in components for automobiles, aircraft, etc.
  • open-cell ceramic foams can be prepared from an open-cell, hydrophilic flexible organic foam material having a plurality of interconnected voids surrounded by a web of the foam material.
  • the organic foam material is impregnated with an aqueous ceramic slurry so that the web is coated, and the voids are filled, with slurry. Then the slurry-impregnated material is compressed to expel 20-75% of the slurry, and the pressure thereafter is released so that the web remains coated with slurry.
  • the material After drying, the material is heated, first to burn out the flexible organic foam and then to sinter the ceramic coating, thereby leaving a consolidated ceramic foam having a plurality of interconnected voids surrounded by a web of bonded or fused ceramic in the configuration of the precursor organic foam.
  • a metal, metal/ceramic, and/or ceramic coating is applied to a foamed polyurethane sponge via an electroconducting film (e.g., electroless nickel or copper plating) previously applied to the sponge.
  • a galvanic coating is described as being applied over the electroconducting film, followed by a molten-spray coating of metal/ceramic or ceramic applied by means of a 10,000-15,000°C argon plasma flame.
  • the final web is described as being hollow and multi-layered in structure and gradually changing from metallic on the inside to an external ceramic character.
  • the molten-spray coating technique is stated to be applicable only to sponges no thicker than 12 mm if the spray can be applied on one face only, and no thicker than 25 mm if spraying can be applied to two opposite sides.
  • Sowards had disclosed a method of making thin-walled alumina-containing structures by firing, in an oxygen-containing atmosphere, thin aluminum sections (such as cans, tubes, boxes, arrays of tubes, honeycombs, etc., or crumpled forms, made from aluminum sheets or formed by extrusion methods), coated with an oxide of an alkali metal, alkaline earth metal, vanadium, chromium, molybdenum, tungsten, copper, silver, zinc, antimony, or bismuth, or precursor thereof as a fluxing agent, and, optionally, a particulate filler refractory.
  • thin aluminum sections such as cans, tubes, boxes, arrays of tubes, honeycombs, etc., or crumpled forms, made from aluminum sheets or formed by extrusion methods
  • an oxide of an alkali metal, alkaline earth metal, vanadium, chromium, molybdenum, tungsten, copper, silver, zinc, antimony, or bismuth, or precursor thereof as a fluxing agent and,
  • the process was reported to form double-walled sections of refractory having a sheet-like void near the center, said to have resulted from the migration of molten aluminum through fissures in the oxide film formed on the surface of the metal.
  • Oberlin showed this structure to be weak, and described eliminating the double-walled structure by using a vanadium compound and a silicate fluxing agent in the process. Sowards pre-coated the structure with aluminum powder prior to firing, thereby producing the double-walled structure with thicker walls. Only aluminum template structures fabricated from sheets or formed by extrusion were contemplated.
  • the interconnected walls of a honeycomb define closed cells or channels longitudinally extending the entire length of the walls.
  • the channels are aligned so as to be parallel to a single common axis, a structure which is less useful for certain purposes than that of open-cell foams, in which the cellular structure is three-dimensional.
  • the particulate collecting efficiency of a ceramic honeycomb filter disposed in an exhaust passage of a diesel engine has been reported to be low (U.S. Patent 4,540,535), and honeycomb catalyst supports have been reported as suffering from a relatively low geometric area and undesirably low turbulence (U.S. Patent 3,972,834).
  • oxidation has been considered in its broadest sense, to mean one or more metals giving up electrons to, or sharing electrons with, another element or combination of elements to form a compound. Accordingly, the term "oxidant" denotes an electron acceptor or sharer.
  • ceramic composite products are produced by growing a ceramic product in a bed of filler material adjacent to a body of molten parent metal.
  • the molten metal reacts with a gaseous oxidant, such a oxygen, which has been allowed to permeate the filler bed.
  • the resultant oxidation reaction product e.g. alumina, can grow into and through the mass of filler as molten parent metal is drawn continuously through fresh oxidation reaction product.
  • the filler particles are embedded within the polycrystalline ceramic product comprising the oxi dation reaction product interconnected in three dimensions.
  • the resultant oxidation reaction product e.g. alumina
  • the resultant oxidation reaction product can grow into and through the mass of filler as molten parent metal is drawn through fresh oxidation reaction product.
  • the molten metal in the space originally occupied by the metal mold has been consumed, there remains a cavity that inversely replicates the shape of geometry of the original metal mold, with the cavity being surrounded by the resulting ceramic composite.
  • Ceramic foams have a distinctive physical structure which imparts many beneficial properties and uses thereto. This structure is characterized by open cells or channels interconnected randomly in three dimensions, affording a high surface area per unit volume and high strength-to-weight ratio. Turbulent fluid flow results from these three-dimensional cellular structures, which can be advantageous in some applications, and is in contrast to the laminar flow in a honeycomb. A need exists for improvements in such products, and in methods of making them.
  • the present invention provides a ceramic foam comprising a reticulated body of open cells or open channels which are interconnected randomly in three dimensions, and a substantially continuous ceramic material.
  • a metallic foam is utilized as precursor metal from which is derived an oxidation reaction product.
  • the foam is a reticulated body of interlacing ligaments, veins, fibers, ribbons, or the like, of precursor metal interconnected randomly in three dimensions thereby defining open cells or channels.
  • the channels, as defined by the external surfaces of the ligaments, likewise are interconnected randomly in three dimensions.
  • the metal reticulum serves as the precursor metal or parent metal, and it is at least partially consumed in the formation of oxidation reaction product.
  • the reticulated body of parent metal is first treated in a manner such that a support coating, capable per se of maintaining the integrity of the open-cell structure of the body under the process conditions, forms on the surfaces of ligaments at a temperature below the melting point of the metal.
  • This support coating may be intrinsically formed or be externally applied, as described below in detail.
  • the coated parent metal body is then heated at a temperature above the melting point of the metal whereby molten metal contacts and reacts with an oxidant and forms an oxidation reaction product.
  • the process conditions are maintained to draw parent metal through the oxidation reaction product which, on contact with the oxidant, forms additonal oxidation reaction product.
  • the process is continued until the desired coating of polycrystalline ceramic is formed, which comprises oxidation reaction product and, optionally, metallic constituents and/or pores.
  • the ceramic foam product comprises an open-cell, reticulated ceramic structure, and substantially all or only part of the metallic ligaments may be consumed in the process.
  • the foam metal ligaments are pre-coated with a permeable layer of filler material which is substantially inert under the process conditions.
  • the resultant ceramic oxidation reaction product e.g. alumina
  • infiltrates and grows into and through the permeable layer as molten metal is drawn through fresh oxidation reaction product.
  • the matrix is comprised of a three-dimensionally interconnected polycrystalline material of oxidation reaction product and filler material, and further may include metallic constituents such as nonoxidized parent metal and/or pores.
  • the oxidation reaction product is interconnected in three dimensions.
  • the metal component may be interconnected or isolated. Likewise, the pores may be interconnected or isolated.
  • the product of the invention comprises a reticulated body of open cells interconnected randomly in three dimensions defined by a substantially continuous ceramic matrix having the structure of interlaced, three-dimensionally, randomly interconnected hollow ligaments or tubules.
  • the hollow ligaments may be substantially empty of parent metal, or may be partially filled with parent metal thereby providing a metal core for the ceramic matrix.
  • both empty and metal-containing hollow ligaments may be present in the ceramic foam product.
  • the ceramic article substantially replicates the configuration of the original metal cellular body thereby producing an article of near net shape. In this way, a ceramic product of desired near net shape, as well as tailored density, composition and properties may be achieved.
  • the relatively simple and limited number of processing steps lends itself to the production of high-purity ceramic bodies and further eliminates many conventional processing defects.
  • the metallic component in the wall portion of the hollow ligaments, and also the metal core may be desirable for uses in which thermal or electrical conductivity are required, e.g., for heat exchangers, heating elements, etc. Also, the metal can improve the strength or toughness, which may be of value in filters, strainers, etc.
  • Ceramic is not to be unduly construed as being limited to a ceramic body in the classical sense, that is, in the sense that it consists entirely of non-metallic and inorganic materials, but rather refers to a body which is predominantly ceramic with respect to either composition or dominant properties, although the body may contain minor or substantial amounts of one or more metallic constituents and/or porosity (interconected and isolated) derived from the parent metal, or reduced from the oxidant or a dopant, most typically within a range of from about 1-40% by volume, but may be higher.
  • “Foam” as applied to both the precursor metal or to the product refers to a self-supporting body possessing a cellular, skeletal, web-like structure.
  • Oxidation reaction product generally means one or more metals in any oxidized state wherein a metal has given up electrons to or shared electrons with another element, compound, or combination thereof. Accordingly, an “oxidation reaction product” under this definition includes the product of reaction of one or more metals with an oxidant, such as those described in this application.
  • Oxidant means one or more suitable electron acceptors or electron sharers and may be solid, a liquid or a gas (vapor) or some combination of these (e.g., a solid and a gas) at the process conditions.
  • Parent metal is intended to refer to relatively pure metals, commercially available metals with impurities and/or alloying constituents therein, and alloys and intermetallic compounds of the metals. When a specific metal is mentioned, the metal identified should be rea d with this definition in mind unless indicated otherwise by the context.
  • the formation and growth of the ceramic product is carried out on an open-cell parent metal body having a three-dimensional cellular structure, i.e., a metal foam or sponge.
  • a metal foam or sponge Because of the complexity of this structure, the limited accessibility to its interior surfaces, and the fineness of the supporting structure, special conditions are required to accomplish the conversion of an open-cell metal body to an open-cell ceramic body by the growth process.
  • the open-cell parent metal body serves as a pattern or mold for the formation of a similarly configured ceramic foam body. Despite the structural complexity of the parent metal body, and the molten condition and displacement of the metal during the process, the integrity and configuration of the original open-cell structure of the parent metal body is substantially retained.
  • the present invention provides this advantage in forming shaped ceramic bodies in that the metal foam can be readily shaped, including forming cavities, in contrast to machining the finished ceramic article, which is more difficult and costly.
  • the outside dimensions and configuration of the metal foam are substantially replicated by the finished ceramic because the metal ligament or vein has a relatively small cross-sectional dimension and therefore growth of the oxidation reaction product does not substantially alter the dimensions of the body.
  • the parent metal body is first treated to produce a support coating on the metal ligaments, which coating, per se , maintains the integrity of the open-cell structure.
  • the support coating may be permeable to the gaseous oxidant if used, or contains a solid or liquid oxidant, and permits infiltration and growth of an oxidation reaction product.
  • This treatment to provide a support coating is below the melting point of the parent metal, and treatment can be accomplished in any one of various ways.
  • the support coating is intrinsically formed by oxidation of the precursor metal below its melting point to form a layer of oxidation reaction product. In the intrinsic forming of the support coating, it is preferable to conduct the heat-up to the low temperature region at a slow rate.
  • the metal foam can be heated to the low temperature at a relatively rapid rate and then soaked at the required temperature for sufficient time to form the coating.
  • the preheat step alone is acceptable.
  • the metal foam comprises 6101 aluminum alloy
  • a sufficient support coating is formed comprising a thin support coating of aluminum oxide.
  • relatively pure aluminum is heated in a nitrogen atmosphere at 650°C for several hours, a thin support coating of aluminum nitride is formed, as illustrated in Example 11 below.
  • This support coating should be of sufficient thickness to support and maintain the integrity and configuration of the original metal foam structure.
  • the foam will not collapse because of the support coating.
  • the oxidation reaction process proceeds, and oxidation reaction product is grown or developed to the desired thickness for the ceramic foam product.
  • a material, or its precursor which reacts or is decomposable below the metal's melting point to form a permeable support coating, is applied to the foam metal surfaces prior to heating.
  • the support coating can form during ramp heat-up from a temperature below the melting point of the parent metal to a temperature above its melting point, without the need for a hold-time at the premelting temperature.
  • coating materials, or their precursors, particularly useful with an aluminum parent metal system are metallic salts and compounds, including organometallic compounds, of alkali, alkaline-earth and transition metals, and slurries or slips of alumina, very fine aluminum powder, silica, silicon carbide, aluminum nitride, silicon nitride, boron carbide, or any combination thereof.
  • a dopant material may be used in conjunction with the metal, as described below in detail.
  • fillers may be applied to the surfaces of the metal ligaments so that a ceramic composite is formed.
  • Suitable fillers may include the carbides of silicon, aluminum, boron, hafnium, niobium, tantalum, thorium, titanium, tungsten, vanadium, and zirconium; the nitrides of silicon, aluminum, boron, hafnium, niobium, tantalum, thorium, titanium, uranium, vanadium, and zirconium; the borides of chromium, hafnium, molybdenum, niobium, tantalum, titanium, tungsten, vanadium, and zirconium; and the oxides of aluminum, beryllium, cerium, chromium, hafnium, iron, lanthanum, magnesium, nickel, titanium, cobalt, manganese, thorium, copper, uranium, yttrium, zirconium, and silicon.
  • the temperature of the parent metal is raised to a region above its melting point but below the melting point of the oxidation reaction product.
  • this temperature interval may range from about 690-1450°C, and preferably 900-1350°C.
  • the molten metal adjacent the coating reacts with the oxidant, which in the case of a gas has permeated the coating, or with any solid and/or liquid oxidant present in the support coating.
  • oxidation reaction product is formed when molten parent metal contacts the oxidant, and molten metal will be drawn through the newly formed oxidation reaction product to cause the formation and continued growth of oxidation reaction product at the surface exposed to the oxidant.
  • the metal originally present as the precursor metal may be essentially completely transported out of its original location (ligaments enveloped by the support coating) so that the resulting product comprises randomly interconnected ceramic hollow ligaments or tubules having a bore of substantially the same size (diameter) as that of the original metal ligament.
  • the ceramic tubules or hollow ligaments comprise a polycrystalline material consisting essentially of oxidation reaction product and optionally metallic constituents and/or pores. If the process is conducted to convert substantially all of the parent metal to oxidation reaction product, interconnected porosity will develop in place of the interconnected metallic component, and there may still be isolated metal and/or pores.
  • a portion only of the molten metal may be converted into the oxidation reaction product, and a core of re-solidified parent metal will remain in the tubules or hollow ligaments.
  • FIG. 1 there is shown a metal sponge, indicated generally by the numeral 1 , having ligaments or veins 2 .
  • a coating 4 has been applied to a portion of the ligaments interconnected to form a three-dimensional reticulated structure having open cells 3 , which interconnect randomly in three dimensions by virtue of the three-dimensional ligament structure.
  • Cells 3 are generally polygonal in shape, but may be non-angular. e.g. oval or circular.
  • FIG. 2 shows the ceramic product made in accordance with the invention, and shows hollow ligaments or tubules 5 of ceramic material and open cells 3 '.
  • the ceramic ligaments 5 shown in cross-section in FIGS. 2 and 2A are substantially hollow, the toroidal surface formed by sectioning through the walls of said tubules being denoted by the numeral 6 .
  • These tubules have hollow bores 7, which can add to the lightness of the product as well as its surface area per unit volume.
  • the tubule shown in FIG. 2B has a ceramic wall 6 and a metal core 8 resulting from incomplete conversion of the parent metal to the oxidation reaction product. Also, the metal core typically does not completely fill the interior of the ligament, resulting in some void volume 7 .
  • a particularly useful metal foam as the precursor metal for use in the present process is the metal foam known as Duocel, a product of Energy Research and Generation, Inc., Oakland, California, USA. This product is described as a foam metal having a reticulated structure of open, dodecahedronal-shaped cells connected by continuous, solid-metal ligaments. It should be understood, however, that the source and form of the precursor metal is not essential to the practice of the invention so long as it is cellular in structure.
  • One means in producing a suitable metal foam is to cast molten metal with an expandable or fugitive material. For example, molten aluminum is cast around granules of salt, or around particles of coke such as used in fluidized beds.
  • a metal foam may comprise a consolidated mass of metal fibers of desired bulk density to provide an open network of interstitial voids.
  • Aluminum is a preferred parent metal for use in the present process. It is readily available in foam metal form, such as Duocel, and is particularly well-adapted for use in processes wherein a molten parent metal is to be drawn into, or through, an oxidation reaction product for reacting with an oxidant.
  • parent metals other than aluminum can be employed in these ceramic growth processes, and these include such metals as titanium, tin, zirconium, and hafnium. All such metals can be used in the present process if they are available, or can be made available, in open-cell, i.e., foam, metal form.
  • the molten metal usually will be heated in a reactive atmosphere, e.g., air or nitrogen in the case of aluminum.
  • a reactive atmosphere e.g., air or nitrogen in the case of aluminum.
  • the support coating is gas-permeable so that upon exposure of the coated precursor to the atmosphere, the gas permeates the coating to contact the molten parent metal adjacent thereto.
  • a solid oxidant may be employed by dispersing it through the precursor material for the support coating.
  • a solid oxidant may be particularly useful in forming the support coating or in forming a relatively thin ceramic matrix.
  • a solid, liquid or vapor-phase oxidant, or a combination of such oxidants may be employed, as noted above.
  • typical oxidants include, without limitation, oxygen, nitrogen, a halogen, sulphur, phosph orus, arsenic, carbon, boron, selenium, tellurium, and compounds and combinations thereof, for example, methane, ethane, propane, acetylene, ethylene, propylene (the hydrocarbon as a source of carbon), and mixtures such as air, H2/H2O and CO/CO2, the latter two (i.e., H2/H2O and CO/CO2) being useful in reducing the oxygen activity of the environment.
  • a vapor-phase oxidant is preferred, but it should be understood that two or more vapor-phase oxidants may be used in combination. If a vapor-phase oxidant is used in conjunction with a material for the support coating which may include a filler, the coating is permeable to the vapor-phase oxidant so that upon exposure to the oxidant, the vapor-phase oxidant permeates the coating to contact the molten parent metal.
  • vapor-phase oxidant means a vaporized or normally gaseous material which provides an oxidizing atmosphere.
  • oxygen or gas mixtures containing oxygen are preferred vapor-phase oxidants, as in the case where aluminum is the parent metal, with air usually being more preferred for obvious reasons of economy.
  • an oxidant is identified as containing or comprising a particular gas or vapor, this means an oxidant in which the identified gas or vapor is the sole, predominant or at least a significant oxidizer of the parent metal under the conditions obtaining in the oxidizing environment utilized.
  • the major constituent of air is nitrogen
  • the oxygen content of air is the sole oxidizer for the parent metal because oxygen is a significantly stronger oxidant than nitrogen.
  • Air therefore falls within the definition of an "oxygen-containing gas” oxidant but not within the definition of a "nitrogen-containing gas” oxidant.
  • An example of a "nitrogen-containing gas” oxidant as used herein and in the claims is "forming gas", which typically contains about 96 volume percent nitrogen and about 4 volume percent hydrogen.
  • a solid oxidant When a solid oxidant is employed in conjunction with the support coating, it is usually dispersed through the coating, or its precursor and also filler if used, in the form of particulates, or perhaps as coatings on the filler particles.
  • Any suitable solid oxidant may be employed including elements, such as boron or carbon, or reducible compounds, such as silicon dioxide or certain borides of lower thermodynamic stability than the boride reaction product of the parent metal.
  • reducible compounds such as silicon dioxide or certain borides of lower thermodynamic stability than the boride reaction product of the parent metal.
  • the resulting oxidation reaction product is aluminum boride.
  • the oxidation reaction may proceed so rapidly with a solid oxidant that the oxidation reaction product would tend to fuse due to the exothermic nature of the process. Such an occurrence could degrade the microstructural uniformity of the ceramic body.
  • This rapid exothermic reaction is avoided by mixing into the composition a relatively inert filler which exhibits low reactivity.
  • a suitable inert filler is one which is identical to the intended oxidation reaction product.
  • a liquid oxidant in conjunction with the support coating and the filler, the entire coating or filler may be impregnated with the oxidant.
  • a liquid oxidant means one which is a liquid under the oxidation reaction conditions and so a liquid oxidant may have a solid precursor, such as a salt, which is molten at the oxidation reaction conditions.
  • the liquid oxidant may have a liquid precursor, e.g., a solution of a material which is melted or decomposed at the oxidation reaction conditions to provide a suitable oxidant moiety.
  • liquid oxidants as herein defined include low-melting glasses.
  • certain parent metals under specific conditions of temperature and oxidizin g atmosphere meet the criteria necessary for the ceramic process with no special additions or modifications.
  • dopant materials used in combination with the parent metal can favorably influence or promote the process.
  • the dopant or dopants may be provided as alloying constituents of the parent foam metal, or may be supplied by the support coating. In some instances the dopant may be omitted depending on process temperatures and parent metal.
  • a dopant material is preferred or required if the process temperature is about 1200°C, but no dopant need be used when processing commercially pure aluminum at a temperature of about 1700°C.
  • Useful dopants for an aluminum parent foam metal, particularly with air as the oxidant include, for example, maganesium metal and zinc metal, particularly in combination with other dopants , such as silicon, described below. These metals, or a suitable source of the metals, may be alloyed into the aluminum-based parent foam metal at concentrations for each of between about 0.1 and 10% by weight based on the total weight of the resulting doped metal. The concentration range for any one dopant will depend on such factors as the combination of dopants and the process temperature. Concentrations within this range appear to initiate the ceramic growth from molten metal, enhance metal transport, and favorably influence the growth morphology of the resulting oxidation reaction product.
  • dopants which are effective in promoting ceramic growth from molten metal, for aluminum-based parent metal systems are, for example, silicon, germanium, tin, and lead, especially when used in combination with magnesium or zinc.
  • One of more of these other dopants, or a suitable source of them, is alloyed into the aluminum foam parent metal system at concentrations for each of about from 0.5 to 15% by weight of the total alloy; however, more desirable growth kinetics and growth morphology are obtained with dopant concentrations in the range of about 1-10% by weight of the total parent metal alloy.
  • Lead as a dopant is generally alloyed into the aluminum-based parent metal at a temperature of at least 1000°C so as to make allowances for its low solubility in aluminum; however, the addition of other alloying components, such as tin, will generally increase the solubility of lead and allow the alloying materials to be added at a lower temperature.
  • One or more dopants may be used depending upon the circumstances.
  • particularly useful combinations of dopants include (a) magnesium and silicon or (b) magnesium, zinc and silicon.
  • a preferred magnesium concentration falls within the range of about from 0.1 to 3% by weight, for zinc in the range of about from 1 to 6% by weight, and for silicon in the range of about from 1 to 10% by weight.
  • Useful dopants in forming aluminum nitride include calcium, barium, silicon, magnesium and lithium.
  • dopant materials useful with an aluminum parent metal, include sodium, germanium, tin, lead, lithium, calcium, boron, phosphorus, and yttrium which may be used individually or in combination with one or more dopants depending on the oxidant and process conditions.
  • Sodium and lithium may be used in very small amounts in the parts per million range, typically about 100-200 parts per million, and each may be used alone or together, or in combination with other dopant(s).
  • Rare earth elements such as cerium, lanthanum, praseodymium, neodymium, and samarium are also useful dopants, and herein again especially when used in combination with other dopants.
  • An external dopant may be applied by soaking the parent open-cell metal body in an aqueous solution of a salt of the dopant metal (Example 2), or by dipping the parent open-cell metal body in an organic slurry o f the dopant powder, followed by shaking to disperse the slurry throughout the open-cell skeleton structure.
  • the quantity of external dopant is effective over a wide range relative to the amount of parent metal to which it is applied.
  • the foam metal used as the starting material was a 5.1 cm x 5.1 cm x 2.5 cm block of the previously mentioned Duocel, made, in this case, of 6101 aluminum alloy.
  • the major alloying constituents in this metal are silicon (0.3-0.7%), magnesium (0.35-0.8%), and iron (0.5% maximum).
  • Elements present in amounts of 0.1% or less include copper, zinc, boron, manganese, and chromium.
  • the foam metal is described by the manufacturer as having a reticulated structure of open, duodecahedral-shaped cells connected by continuous, solid aluminum alloy ligaments. Its cell size was 4 pores per centimeter (mean cell size of 0.20cm).
  • the metal foam block was preconditioned by sequential cleaning treatments in acetone and in a 20% aqueous sodium chloride solution for about 2 minutes per treatment. The block then was placed on top of a bed of wollastonite in a refractory crucible.
  • the crucible was placed in a furnace where it was heated in air to a temperature of 600°C over a 2-hour heat-up period, and then maintained at 600°C for 2 hours. This heating step permitted the formation of a permeable coating on the foam metal surfaces sufficient per se to maintain the reticular integrity of the metal block. At this point, the furnace temperature was increased up to 1300°C over a 2.3-hour period, and was maintained there for 15 hours.
  • the sheath comprised a matrix of three-dimensionally interconnected alumina containing dispersed aluminum metal.
  • the core was aluminum.
  • the sheath, i.e., the tubular wall, was hard and electrically conducting.
  • Example 1 The procedure described in Example 1 was repeated with the exception that the preconditioned Duocel block was soaked in a 20% aqueous solution of magnesium nitrate and dried, and the 600°C preheat step was omitted. The coated foam metal was heated in air for 4 hours until a temperature of 1300°C was reached, and then maintained at 1300°C for 15 hours.
  • the external appearance and size of the cooled product were like those of the product formed according to Example 1, but, in this case, the cross-sectional photomicrographs of the web-forming ligaments revealed a tubular structure having a hollow core and a thicker wall than the product described in Example 1.
  • the diameter of the hollow core was essentially the same as that of the ligaments in the Duocel used.
  • the wall consisted essentially of an alumina matrix containing dispersed aluminum metal. A magnesium aluminate spinel also was present.
  • Alumina powder in a 1-5 ⁇ particle size range was slurried in a 20% solution of a nitrile rubber in cyclohexanone.
  • a preconditioned Duocel block such as that described in Example 1 was dipped into the slurry and shaken so as to deposit a permeable layer of alimina on the metal surfaces.
  • the coated block was heated according to the procedure described in Example 2.
  • molten aluminum was drawn into, and oxidized in and adjacent the permeable alumina coating, forming an open-cell product in which the nature of the web-forming ligaments was that of a metal-filled tubular structure, i.e., an aluminum core surrounded by a sheath of an alumina matrix with aluminum metal dispersed therein.
  • the sheath was hard and electronically conducting.
  • the procedure described in Examples 3 was repeated with variations in the compositions of the coatings applied to the Duocel foam block prior to the ceramic-forming heating step.
  • the nature of the ligaments in the resulting ceramic foam was that of a tubular structure, i.e., a tubule of a ceramic composite material which comprised a metal-bearing ceramic matrix having embedded therein, a granular form, the ceramic material(s) present in the support coating.
  • the tubules had metal cores, and, in others, th ey were hollow (with a diameter essentially the same as that of the metal ligaments in the Duocel used), depending on processing time, and whether or not an external dopant (as illustrated in Example 2) had been used.
  • the first aluminum foam preform was prepared by casting molten aluminum around sodium chloride granules and then removing the salt by leaching in water.
  • the second preform was made by pressure casting molten aluminum around fluid coke particles which were subsequently removed by heating in air
  • the porous aluminum foam body was subject to heating in a nitrogen atmosphere.
  • the heating schedule was as follows:

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Catalysts (AREA)
  • Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
  • Porous Artificial Stone Or Porous Ceramic Products (AREA)
EP87630196A 1986-09-16 1987-09-16 Mousses céramiques Expired - Lifetime EP0261070B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT87630196T ATE76050T1 (de) 1986-09-16 1987-09-16 Keramische schaeume.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US90811686A 1986-09-16 1986-09-16
US908116 1986-09-16
US07/089,376 US4808558A (en) 1987-08-26 1987-08-26 Ceramic foams
US89376 1987-08-26

Publications (2)

Publication Number Publication Date
EP0261070A1 true EP0261070A1 (fr) 1988-03-23
EP0261070B1 EP0261070B1 (fr) 1992-05-13

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EP87630196A Expired - Lifetime EP0261070B1 (fr) 1986-09-16 1987-09-16 Mousses céramiques

Country Status (24)

Country Link
EP (1) EP0261070B1 (fr)
JP (1) JP2540560B2 (fr)
KR (1) KR950010001B1 (fr)
CN (1) CN1026687C (fr)
AU (1) AU599142B2 (fr)
BG (1) BG50938A3 (fr)
BR (1) BR8704767A (fr)
CA (1) CA1308888C (fr)
CS (1) CS276945B6 (fr)
DE (1) DE3779028D1 (fr)
DK (1) DK169993B1 (fr)
ES (1) ES2032857T3 (fr)
FI (1) FI90059C (fr)
GR (1) GR3005438T3 (fr)
HU (1) HU203861B (fr)
IE (1) IE61321B1 (fr)
IL (1) IL83853A (fr)
MX (1) MX165373B (fr)
NO (1) NO175303C (fr)
NZ (1) NZ221756A (fr)
PH (1) PH26329A (fr)
PL (1) PL156557B1 (fr)
PT (1) PT85713B (fr)
YU (1) YU171787A (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT395002B (de) * 1988-03-25 1992-08-25 Cabot Corp Keramisches material mit niedriger dielektrizitaetskonstante
EP0844221A1 (fr) * 1996-11-21 1998-05-27 Basf Aktiengesellschaft Produits frittés à porosité ouverte et procédé de leur fabrication
US5976454A (en) * 1996-04-01 1999-11-02 Basf Aktiengesellschaft Process for producing open-celled, inorganic sintered foam products
US6171532B1 (en) 1996-05-17 2001-01-09 Basf Aktiengesellschaft Method of stabilizing sintered foam and of producing open-cell sintered foam parts
US6602449B1 (en) 1998-04-06 2003-08-05 Cellaris Limited Method of producing ceramic foams
WO2017220082A1 (fr) * 2016-06-24 2017-12-28 Otto-Von-Guericke-Universität Magdeburg, Patentwesen Matériau cellulaire et fabrication de ce dernier

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1063410C (zh) * 1996-10-30 2001-03-21 大连理工大学 一种利用自蔓延高温合成控制制备泡沫陶瓷材料的方法
CN1063411C (zh) * 1996-10-30 2001-03-21 大连理工大学 自蔓延高温合成控制制备(Al2O3+TiB2)泡沫陶瓷过滤器的方法
FR2769517B1 (fr) * 1997-10-13 1999-11-12 Francis Al Dullien Separateur de type spongieux en mousse reticulee
DE102004012990A1 (de) * 2004-04-30 2005-11-24 Girlich, Dieter, Dr. Verbundwerkstoff, Verfahren zur Herstellung eines derartigen Verbundwerkstoffes sowie dessen Verwendung
JP5397733B2 (ja) * 2008-03-24 2014-01-22 独立行政法人物質・材料研究機構 昇華性金属元素と酸化性金属元素の合金及び多孔質セラミックの複合体とその製造方法
CN101445381B (zh) * 2008-12-31 2011-06-29 南京航空航天大学 仿毛细血管丛的Al芯/Al2O3基陶瓷鞘自愈合复合泡沫防热结构及其制备方法
DE102012007396B3 (de) * 2012-04-16 2013-06-13 Cast Aluminium Industries Verfahren zur Bildung eines schnell erhärtenden, anorganischen Schaums und reaktives Pulver zur Bildung eines schnell erhärtenden Mineralschaums
US20200239312A1 (en) * 2017-10-02 2020-07-30 Cellmobility, Inc. Method of Making Aluminum Nitride Foam
CN109745907B (zh) * 2017-11-08 2021-05-28 中国科学院金属研究所 一种基于中空泡沫材料的流体分布器及其应用
PT3710407T (pt) * 2017-11-16 2023-08-28 Pontic Tech Llc Aparelho e método de descontaminação de fluidos
CN113308713A (zh) * 2021-05-25 2021-08-27 西部金属材料股份有限公司 一种金属陶瓷阳极及其制备方法和应用

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0155831A2 (fr) * 1984-03-16 1985-09-25 Lanxide Technology Company, Lp. Matériaux céramiques et procédé de sa fabrication
EP0193292A2 (fr) * 1985-02-04 1986-09-03 Lanxide Technology Company, Lp. Corps céramiques composites et leurs procédés de fabrication

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0155831A2 (fr) * 1984-03-16 1985-09-25 Lanxide Technology Company, Lp. Matériaux céramiques et procédé de sa fabrication
EP0193292A2 (fr) * 1985-02-04 1986-09-03 Lanxide Technology Company, Lp. Corps céramiques composites et leurs procédés de fabrication

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT395002B (de) * 1988-03-25 1992-08-25 Cabot Corp Keramisches material mit niedriger dielektrizitaetskonstante
US5976454A (en) * 1996-04-01 1999-11-02 Basf Aktiengesellschaft Process for producing open-celled, inorganic sintered foam products
US6171532B1 (en) 1996-05-17 2001-01-09 Basf Aktiengesellschaft Method of stabilizing sintered foam and of producing open-cell sintered foam parts
EP0844221A1 (fr) * 1996-11-21 1998-05-27 Basf Aktiengesellschaft Produits frittés à porosité ouverte et procédé de leur fabrication
US5998317A (en) * 1996-11-21 1999-12-07 Basf Aktiengesellschaft Open-celled porous sintered products and their production
US6602449B1 (en) 1998-04-06 2003-08-05 Cellaris Limited Method of producing ceramic foams
WO2017220082A1 (fr) * 2016-06-24 2017-12-28 Otto-Von-Guericke-Universität Magdeburg, Patentwesen Matériau cellulaire et fabrication de ce dernier

Also Published As

Publication number Publication date
GR3005438T3 (fr) 1993-05-24
NZ221756A (en) 1990-05-28
IE872486L (en) 1988-03-16
PH26329A (en) 1992-04-29
AU599142B2 (en) 1990-07-12
IE61321B1 (en) 1994-11-02
DK481987D0 (da) 1987-09-15
HU203861B (en) 1991-10-28
PL267778A1 (en) 1988-09-29
CA1308888C (fr) 1992-10-20
MX165373B (es) 1992-11-06
DK169993B1 (da) 1995-04-24
CN87106360A (zh) 1988-04-06
KR880003877A (ko) 1988-05-30
NO873760D0 (no) 1987-09-09
FI90059B (fi) 1993-09-15
JP2540560B2 (ja) 1996-10-02
FI874027A0 (fi) 1987-09-15
CS276945B6 (en) 1992-10-14
BG50938A3 (bg) 1992-12-15
PL156557B1 (pl) 1992-03-31
DK481987A (da) 1988-03-17
EP0261070B1 (fr) 1992-05-13
HUT46632A (en) 1988-11-28
NO175303B (no) 1994-06-20
DE3779028D1 (de) 1992-06-17
PT85713A (en) 1987-10-01
ES2032857T3 (es) 1993-03-01
FI90059C (fi) 1993-12-27
PT85713B (pt) 1990-08-31
IL83853A (en) 1991-11-21
CN1026687C (zh) 1994-11-23
AU7837687A (en) 1988-03-24
IL83853A0 (en) 1988-02-29
NO873760L (no) 1988-03-17
NO175303C (no) 1994-09-28
FI874027A (fi) 1988-03-17
KR950010001B1 (en) 1995-09-04
JPS63129081A (ja) 1988-06-01
YU171787A (en) 1989-04-30
BR8704767A (pt) 1988-05-03
CS8706616A2 (en) 1991-09-15

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